Pyridoxamine 5-prime-phosphate oxidase deficiency: Difference between revisions

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{{SK}} PNPO deficiency; PNPO-related neonatal epileptic encephalopathy; pyridoxamine 5-prime-phosphate oxidase deficiency; pyridoxine-5'-phosphate oxidase deficiency
==Overview==
==Overview==
Pyridoxal 5'-phosphate-dependent epilepsy is a condition that involves seizures beginning soon after birth or, in some cases, before birth. The seizures typically involve irregular involuntary muscle contractions (myoclonus), abnormal eye movements, and convulsions.  Most babies with this condition are born prematurely and may have a temporary, potentially toxic, increase in lactic acid in the blood (lactic acidosis). Additionally, some infants have a slow heart rate and a lack of oxygen during delivery (fetal distress).<ref>http://ghr.nlm.nih.gov/condition/pyridoxal-5-phosphate-dependent-epilepsy</ref>
Pyridoxal 5'-phosphate-dependent epilepsy is a rare condition; approximately 14 cases have been described so far. It is a condition that involves seizures beginning soon after birth or, in some cases, before birth. <ref>http://ghr.nlm.nih.gov/condition/pyridoxal-5-phosphate-dependent-epilepsy</ref>


==References==
==References==

Revision as of 16:31, 2 August 2012

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Synonyms and keywords: PNPO deficiency; PNPO-related neonatal epileptic encephalopathy; pyridoxamine 5-prime-phosphate oxidase deficiency; pyridoxine-5'-phosphate oxidase deficiency

Overview

Pyridoxal 5'-phosphate-dependent epilepsy is a rare condition; approximately 14 cases have been described so far. It is a condition that involves seizures beginning soon after birth or, in some cases, before birth. [1]

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